Establishment registration
Prollenium US
FDA establishment registration 3014151870 · Raleigh, US
Key facts
| Registration number | 3014151870 |
|---|---|
| Establishment name | Prollenium US |
| Owner/operator | Prollenium Medical Technologies Inc. |
| Owner/operator number | 10055618 |
| FEI number | 3014151870 |
| Address | 9121 Anson Way, Suite 213 |
| City | Raleigh |
| State | NC |
| Country | US |
| Registration valid through | 2026 |
At a glance
- 1–9 Device listings
- None UDI devices (GUDID)
- Current Registration current
- None FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database